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Genetic counselling

By Raising Children Network
 
 

If your child is diagnosed with a disability, your doctor may recommend that you get genetic counselling. Many disabilities are genetic, and genetic counselling can teach you more about the diagnosis as well as assess the risk of other family members having the same disability.

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Recent advances in DNA technology and increased public awareness of the links between genetic make-up and many common diseases and disabilities mean more and more people are being referred for genetic counselling every year.

What is genetic counselling?

Genetic counselling is a discussion with a medical professional qualified in genetics. Most people who seek genetic counselling want information, and counselling provides this at a number of stages, before or in conjuction with genetic testing. A counsellor’s first priority is helping you be better informed.

If you have a genetic disorder in the family, counselling will provide an opportunity for you to learn about how it might progress, what some of the consequences could be, the probability of transmitting it and the ways in which this may be prevented. Counselling sessions may include giving you information, helping you to make decisions, and helping you to make adjustments.

Difference between genetic counselling and genetic testing
Genetic counselling consists mainly of communication, education and support, whereas genetic testing is a medical test that is performed on someone who has symptoms or a family history of a genetic disorder. Genetic testing can identify the likelihood of passing on certain genetic diseases or disorders that are caused by an abnormal genetic make-up.

Aims of genetic counselling
If you have a child with a genetic disability, genetic counselling can help you and your family understand the diagnosis and adjust to it. You may want genetic counselling so you can: 

  • understand the medical facts related to your child’s disability – including the diagnosis, the likely cause of the disorder and how it can be managed
  • understand how the child’s heredity may have contributed to the disorder
  • learn more about what the risk is, and how to deal with it if you have more children
  • plan realistically for the future
  • adjust in the most positive ways to the disorder or to the risk of the disorder in another family member.

According to reports from genetic counsellors, some clients seek counselling to confirm what they have learned from the internet. Others want advice on decisions they need to make or support for decisions they have made.

Many people have found genetic counselling from an expert in the field to be very helpful and reassuring.

When to seek genetic counselling

Genetic counselling will help when: 

  • a condition appears to run in the family and there is concern that you or your children may develop it
  • a child in the family has a serious problem that affects growth, development or health, possibly linked with a genetic cause
  • a couple, thinking of having a child, is closely related
  • foetal abnormalities have been detected
  • there is concern that there has been exposure to some chemical or environmental agent that may cause birth defects.

You might also be referred for genetic counselling as part of a medical genetics evaluation to diagnose or manage a genetic disorder.

Preparing for genetic counselling

Before attending a genetic counselling session find out as much as you can about your family’s medical history, because you will be asked to provide detailed information. This might include:

  • your relation to each family member, including whether family members are adopted or half-relatives
  • any major health conditions that affect each family member
  • the age of onset of each condition
  • the cause and age of death of family members (if relevant).

It’s a good idea to write down any questions you think of before going to a session to make sure they are answered.

Genetic counselling: what to expect at a session

During a genetic counselling session, you will speak to a genetic counsellor. The counsellor may:

  • get your family history
  • make or confirm a diagnosis, or let you know that there is no genetic disorder present
  • determine the risk of other family members inheriting the condition you are concerned about
  • discuss the impact and effect of the condition and develop strategies to help you deal with what you've been told
  • refer you to support agencies or other medical professionals
  • give you verbal and written information about the condition.

Further testing may be organised if necessary.

After a counselling session, you should:

  • know more
  • feel emotionally supported because the counsellor has listened to you, validated your concerns, encouraged and understood you
  • have new ways of communicating with your partner and family (sessions are designed to help the whole family)
  • have information and support that will help you make an independent decision about genetically related disorders or treatments
  • have long-term support through an ongoing relationship with the genetic counsellor
  • have guidance that will help you make decisions and deal with possible events in the future and the feelings that come with them.

Following up after a counselling session

Genetic counsellors do not make decisions for you – their role is to give you options and provide support for you as you make a decision. After genetic counselling, you may have to make decisions about:

  • whether or not to have genetic testing done
  • who to tell about the results of the test
  • whether you want medical treatment, if it is available
  • how you are going to live your life in response to the results of the testing
  • how much support you are going to need.

Support

The diagnosis of a genetic condition can place a lot of pressure on a family. Families and individuals who are affected by a genetic condition can find support through a network of contacts at the following organisation:

The Association of Genetic Support of Australasia (AGSA) 
66 Albion St, Surry Hills NSW 2010
Ph: (02) 9211 1462 
Fax: (02) 9211 8077
Email:dianne@agsa-geneticsupport.org.au

AGSA can provide information on genetic support groups across Australasia and help you make contact with families with similar genetic conditions.

Australian genetic testing and counselling services

ACTCanberra Hospital Genetics
PO Box 11, Woden ACT 2606
Ph: (02) 6244 4042 
Fax: (02) 6282 2844
NSWCentre for Genetics Education
PO Box 317, St Leonard NSW 1590
Ph: (02) 9926 7324 
Fax: (02) 9906 7529
Email: genetics@med.usyd.edu.au
NTC/- SA Clinical Genetics Unit
Women’s and Children’s Hospital, North Adelaide SA 5006
Ph: (08) 8161 7375 
Fax: (08) 8161 7010
Email: cywhs.sacgs@cywhs.sa.gov.au
QldQueensland Clinical Genetics service
Royal Children’s Hospital and District Health Service, Herston Qld 4006
Ph: (07) 3636 1686 
Fax: (07) 3636 1987
Email: qcgs@health.qld.gov.au
SASA Clinical Genetics Unit
Women’s and Children’s Hospital, North Adelaide SA 5006
Ph: (08) 8161 7375 
Fax: (08) 8161 6088
Email: cywhs.sacgs@cywhs.sa.gov.au
TasTasmanian Clinical Genetics Service
Royal Hobart Hospital
GPO Box 1060L, Hobart Tas 7001
Ph: (03) 6222 8296 
Fax: (03) 6222 7961
VicGenetic Health Services Victoria
Royal Children’s Hospital, Parkville Vic 3052
Ph: (03) 8341 6201 
Fax: (03) 8341 6390
WAGenetic Services of Western Australia
374 Bagot Rd, Subiaco WA 6008
Phone: (08) 9340 1525 
Fax: (08) 9340 1678

Genetic services in rural and regional Australia

The government has recognised the need for improved access to genetic services in rural, regional and remote areas of Australia and is trying to make more genetic services available.

Check the Centre for Genetics Education for a comprehensive list of services in your area. Contact the genetic service in your capital city and ask about services available to you.

 
 
 
  • Last reviewed21-09-2007
  • References

    Adams, A. (2003). Resources: What is genetic counselling? Retrieved June 8, 2007, from www.genetichealth.com

    Bernhardt, B., Biessecker, B., & Mastromarion, C. (2000). Coals, benefits, and outcomes of genetic counselling: Client and genetic counsellor assessment. American Journal of Medical Genetics, 94, 189-197.

    Biesecker, B., & Peters, K. (2001). Process studies in genetic counselling: Peering into the black box. American Journal of Medical Genetics, 106, 191-198.

    Biotechnology Online. (n.d.). Genetic testing. Retrieved June 18, 2007, from www.biotechnologyonline.gov.au/human/gentesting.cfm

    Macleod, R., Craufurd, D., & Booth, K. (2002). Patients' perceptions of what makes genetic counselling effective: An interpretive phenomenological analysis. Journal of Health Psychology, 7(2), 145-156.

    Pagon, R. (2002). Genetic testing for disease susceptibilities: consequences for genetic counselling. Trends in Molecular Medicine, 8(6), 306-307.

    Pilnick, A., & Dingwall, R. (2000). Research directions in genetic counselling: a review of the literature. Patient Education and Counselling, 44, 95-105.

    Redfearn, M., & Fogarty, M. (2003). Resources: How to find a genetic counsellor. Retrieved June 8, 2007, from www.genetics.com.au

    The Centre for Genetic Education. (2004a). Genetic fact sheet: Genetic testing and screening I - Medical applications. Retrieved June 15, 2007 from www.genetics.com.au.

    The Centre for Genetic Education. (2004b). Genetic fact sheet: Prenatal testing and screening for fetal abnormalities. Retrieved June 15, 2007, from www.genetics.com.au.

    The Centre for Genetics Education. (2005). Genetics fact sheet: Genetic counselling. Retrieved June 8, 2007, from www.genetics.com.au.

    Wang, C., Gonzalez, R., & Merajver, S. (2004). Assessment of genetic testing and related counselling services: current research and future directions. Social Science and Medicine, 58, 1427-1442.

  • Acknowledgements

    Content funded by NSW Department of Ageing, Disability and Home Care